Nucleus basalis magnocellularis and hippocampus are the major sites of FMR-1 expression in the human fetal brain (Q48275073)

10 February 2018

title

Nucleus basalis magnocellularis and hippocampus are the major sites of FMR-1 expression in the human fetal brain (English)

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10 February 2018

author name string

Abitbol M

1

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10 February 2018

Menini C

2

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10 February 2018

Delezoide AL

3

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10 February 2018

Rhyner T

4

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10 February 2018

Vekemans M

5

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10 February 2018

Mallet J

6

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10 February 2018

language of work or name

English

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publication date

1 June 1993

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10 February 2018

published in

Nature Genetics

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10 February 2018

volume

4

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10 February 2018

issue

2

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10 February 2018

page(s)

147-153

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10 February 2018

Variation of the CGG repeat at the fragile X site results in genetic instability: Resolution of the Sherman paradox

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

Direct diagnosis by DNA analysis of the fragile X syndrome of mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

Absence of expression of the FMR-1 gene in fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

Abnormal pattern detected in fragile-X patients by pulsed-field gel electrophoresis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

Fragile X syndrome without CCG amplification has an FMR1 deletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

A point mutation in the FMR-1 gene associated with fragile X mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

A recombination-based assay demonstrates that the fragile X sequence is transcribed widely during development

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

Tissue specific expression of FMR-1 provides evidence for a functional role in fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

Histoanatomic observations of the brain in early infantile autism

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

Central cholinergic pathways in the rat: an overview based on an alternative nomenclature (Ch1-Ch6).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

Cortical effects of neurotoxic damage to the nucleus basalis in rats: persistent loss of extrinsic cholinergic input and lack of transsynaptic effect upon the number of somatostatin-containing, cholinesterase-positive, and cholinergic cortical neuro

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

Amyotrophic lateral sclerosis in a patient with fragile X syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

The Fra(X) syndrome: neurological, electrophysiological, and neuropathological abnormalities

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

Fragile X family with unusual digital and facial abnormalities, cleft lip and palate, and epilepsy

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

Fragile X genotype characterized by an unstable region of DNA.

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

Physical mapping across the fragile X: hypermethylation and clinical expression of the fragile X syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

Methylation analysis of CGG sites in the CpG island of the human FMR1 gene

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

Fifth international workshop on fragile X and X-linked mental retardation

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

Analysis of full fragile X mutations in fetal tissues and monozygotic twins indicate that abnormal methylation and somatic heterogeneity are established early in development

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

Genotype mosaicism in fragile X fetal tissues

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

Isolation of sequences that span the fragile X and identification of a fragile X-related CpG island

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

Adult fragile X syndrome. Clinico-neuropathologic findings

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

Neuropathological findings in primary generalized epilepsy: a study of eight cases

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

Infantile spasms: I. PET identifies focal cortical dysgenesis in cryptogenic cases for surgical treatment

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

Neuronal Migration Disorders: A Contribution of Modern Neuroimaging to the Etiologic Diagnosis of Epilepsy

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

Focal neuronal migration disorders and intractable partial epilepsy: a study of 30 patients

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

Focal neuronal migration disorders and intractable partial epilepsy: results of surgical treatment

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

An analysis of autism in fifty males with the fragile X syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

Epileptic seizures and fra(X) syndrome

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

Epilepsy and fragile X syndrome: a follow-up study

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

Infantile autism--fragile X: molecular findings support genetic heterogeneity

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

Cholinergic innervation of cortex by the basal forebrain: cytochemistry and cortical connections of the septal area, diagonal band nuclei, nucleus basalis (substantia innominata), and hypothalamus in the rhesus monkey

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

Evidence for a cholinergic projection to neocortex from neurons in basal forebrain

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

Cognitive profiles associated with the fra(X) syndrome in males and females.

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

Neuropsychological, psychiatric, and physical manifestations in 149 members from 18 fragile X families

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

Short-term memory and cognitive variability in adult fragile X females.

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

The generation of neuronal diversity in the central nervous system

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

Neuroanatomy of fragile X syndrome: the posterior fossa

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

In situ hybridization histochemistry for the analysis of gene expression in the endocrine and central nervous system tissues: a 3-year experience

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

Modulation of tyrosine hydroxylase gene expression in the central nervous system visualized by in situ hybridization

1 reference

https://api.crossref.org/works/10.1038%2FNG0693-147

7 January 2021

Identifiers

DOI

10.1038/NG0693-147

1 reference

10 February 2018

1 reference

10 February 2018